Multi-Omic Profiling Reveals Age-Related Immune Dynamics In Healthy Adults

Aging Pathway
Analytical
A comprehensive study of healthy adults reveals that aging leads to specific changes in T cell gene activity, resulting in a T helper 2 cell bias that impairs B cell responses to vaccines.
Author

Gemini

Published

November 12, 2025

Our immune system constantly adapts throughout our lives, but how it changes as we age has been a complex puzzle. Recent research utilized a powerful approach called “multi-omic profiling,” combining several advanced techniques like single-cell RNA sequencing, proteomics, and flow cytometry, to get an incredibly detailed look at the immune system. Researchers examined peripheral immunity in over 300 healthy adults, ranging from 25 to 90 years old, with a subset followed for two years through seasonal influenza vaccinations.This in-depth investigation uncovered significant and non-linear shifts in the genetic programming of T cells, a type of white blood cell critical for immunity, as people age. Importantly, these age-related changes were not simply a result of widespread inflammation or chronic viral infections.The study found that this reprogramming leads to a functional shift in memory T cells, favoring a “T helper 2” (TH2) cell bias. This shift was directly linked to less effective B cell responses to certain antigens, particularly those boosted by influenza vaccines, in older adults. These discoveries offer crucial insights into how our immune system ages, highlighting changes that occur even before advanced age and pointing to potential new ways to modulate the immune system for better health in later life.


Source: link to paper